Colon Cancer: Gene >> DEK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397239
Start	18255780:18255780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524T>G
AA Mutation	p.Leu175Arg(p.L175R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397239
Start	18255828:18255828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476G>A
AA Mutation	p.Ser159Asn(p.S159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397239
Start	18236502:18236502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397239
Start	18249831:18249831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769074388
CDS Mutation	c.582G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397239
Start	18258019:18258019(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.291delT
AA Mutation	p.Leu98Ter(p.L98*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397239
Start	18263957:18263957(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.31delG
AA Mutation	p.Glu11ArgfsTer53(p.E11Rfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397239
Start	18226177:18226177(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1113delA
AA Mutation	p.Glu372SerfsTer2(p.E372Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397239
Start	18256402:18256402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.411delA
AA Mutation	p.Gly138GlufsTer12(p.G138Efs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DEK

No Mutation Annotation!